Primary Site >> Stomach Cancer
Gene >> NAGA
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000396398 |
| Start | 42062841:42062841(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.943C>A |
| AA Mutation | p.Arg315Ser(p.R315S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000396398 |
| Start | 42065848:42065848(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.649G>T |
| AA Mutation | p.Asp217Tyr(p.D217Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000396398 |
| Start | 42062963:42062963(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs564028305 |
| CDS Mutation | c.821C>T |
| AA Mutation | p.Thr274Met(p.T274M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000396398 |
| Start | 42067255:42067255(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149600926 |
| CDS Mutation | c.360G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000396398 |
| Start | 42068545:42068545(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.46C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000396398 |
| Start | 42067219:42067219(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.396C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000396398 |
| Start | 42062946:42062946(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs780336867 |
| CDS Mutation | c.838delC |
| AA Mutation | p.Leu280SerfsTer2(p.L280Sfs*2) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |